US20100273689A1 - Lithium hydroxide composition, a process for preparing a lithium hydroxide composition, and a process for using a lithium hydroxide composition - Google Patents
Lithium hydroxide composition, a process for preparing a lithium hydroxide composition, and a process for using a lithium hydroxide composition Download PDFInfo
- Publication number
- US20100273689A1 US20100273689A1 US12/595,138 US59513808A US2010273689A1 US 20100273689 A1 US20100273689 A1 US 20100273689A1 US 59513808 A US59513808 A US 59513808A US 2010273689 A1 US2010273689 A1 US 2010273689A1
- Authority
- US
- United States
- Prior art keywords
- lithium hydroxide
- composition
- hydroxide composition
- fatty acid
- weight percent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 title claims abstract description 634
- 239000000203 mixture Substances 0.000 title claims abstract description 193
- 238000000034 method Methods 0.000 title claims abstract description 41
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 10
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 58
- 239000000194 fatty acid Substances 0.000 claims abstract description 58
- 229930195729 fatty acid Natural products 0.000 claims abstract description 58
- 239000000344 soap Substances 0.000 claims abstract description 56
- 239000012141 concentrate Substances 0.000 claims abstract description 54
- 239000004519 grease Substances 0.000 claims abstract description 51
- 239000002199 base oil Substances 0.000 claims abstract description 37
- -1 fatty acid salt Chemical class 0.000 claims abstract description 34
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 34
- GLXDVVHUTZTUQK-UHFFFAOYSA-M lithium hydroxide monohydrate Substances [Li+].O.[OH-] GLXDVVHUTZTUQK-UHFFFAOYSA-M 0.000 claims description 28
- PQVSTLUFSYVLTO-UHFFFAOYSA-N ethyl n-ethoxycarbonylcarbamate Chemical compound CCOC(=O)NC(=O)OCC PQVSTLUFSYVLTO-UHFFFAOYSA-N 0.000 claims description 27
- 229940040692 lithium hydroxide monohydrate Drugs 0.000 claims description 27
- 238000010438 heat treatment Methods 0.000 claims description 25
- 239000002480 mineral oil Substances 0.000 claims description 17
- 239000000725 suspension Substances 0.000 claims description 8
- 125000005456 glyceride group Chemical group 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 3
- 239000004359 castor oil Substances 0.000 description 17
- 235000019438 castor oil Nutrition 0.000 description 17
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 17
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 16
- 229910052744 lithium Inorganic materials 0.000 description 16
- 239000000654 additive Substances 0.000 description 13
- ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 230000008901 benefit Effects 0.000 description 9
- 235000010446 mineral oil Nutrition 0.000 description 9
- 239000003921 oil Substances 0.000 description 9
- 235000019198 oils Nutrition 0.000 description 9
- 238000003860 storage Methods 0.000 description 9
- 239000002518 antifoaming agent Substances 0.000 description 8
- 229910003002 lithium salt Inorganic materials 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- 229940114072 12-hydroxystearic acid Drugs 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 238000005187 foaming Methods 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 4
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 125000003710 aryl alkyl group Chemical group 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- USOPFYZPGZGBEB-UHFFFAOYSA-N calcium lithium Chemical compound [Li].[Ca] USOPFYZPGZGBEB-UHFFFAOYSA-N 0.000 description 3
- 239000008139 complexing agent Substances 0.000 description 3
- 230000018044 dehydration Effects 0.000 description 3
- 238000006297 dehydration reaction Methods 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 238000005086 pumping Methods 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 235000021314 Palmitic acid Nutrition 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000012990 dithiocarbamate Substances 0.000 description 2
- VKOBVWXKNCXXDE-UHFFFAOYSA-N icosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCC(O)=O VKOBVWXKNCXXDE-UHFFFAOYSA-N 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 230000001050 lubricating effect Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 230000003472 neutralizing effect Effects 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- WMYJOZQKDZZHAC-UHFFFAOYSA-H trizinc;dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S WMYJOZQKDZZHAC-UHFFFAOYSA-H 0.000 description 2
- 239000004711 α-olefin Substances 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- OFOWUDSDZLONKT-UHFFFAOYSA-N 12-oxo-octadecanoic acid Chemical compound CCCCCCC(=O)CCCCCCCCCCC(O)=O OFOWUDSDZLONKT-UHFFFAOYSA-N 0.000 description 1
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 239000004129 EU approved improving agent Substances 0.000 description 1
- 239000005069 Extreme pressure additive Substances 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical compound C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- XYRMLECORMNZEY-UHFFFAOYSA-B [Mo+4].[Mo+4].[Mo+4].[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S Chemical compound [Mo+4].[Mo+4].[Mo+4].[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S XYRMLECORMNZEY-UHFFFAOYSA-B 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000007866 anti-wear additive Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- SAOKZLXYCUGLFA-UHFFFAOYSA-N bis(2-ethylhexyl) adipate Chemical compound CCCCC(CC)COC(=O)CCCCC(=O)OCC(CC)CCCC SAOKZLXYCUGLFA-UHFFFAOYSA-N 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000000881 depressing effect Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- VJHINFRRDQUWOJ-UHFFFAOYSA-N dioctyl sebacate Chemical compound CCCCC(CC)COC(=O)CCCCCCCCC(=O)OCC(CC)CCCC VJHINFRRDQUWOJ-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 150000004659 dithiocarbamates Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 235000021323 fish oil Nutrition 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000000383 hazardous chemical Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 159000000002 lithium salts Chemical group 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000006078 metal deactivator Substances 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- YCWSUKQGVSGXJO-NTUHNPAUSA-N nifuroxazide Chemical group C1=CC(O)=CC=C1C(=O)N\N=C\C1=CC=C([N+]([O-])=O)O1 YCWSUKQGVSGXJO-NTUHNPAUSA-N 0.000 description 1
- 150000002829 nitrogen Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920013639 polyalphaolefin Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920013636 polyphenyl ether polymer Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- WSFQLUVWDKCYSW-UHFFFAOYSA-M sodium;2-hydroxy-3-morpholin-4-ylpropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN1CCOCC1 WSFQLUVWDKCYSW-UHFFFAOYSA-M 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- RIUWBIIVUYSTCN-UHFFFAOYSA-N trilithium borate Chemical compound [Li+].[Li+].[Li+].[O-]B([O-])[O-] RIUWBIIVUYSTCN-UHFFFAOYSA-N 0.000 description 1
- IKXFIBBKEARMLL-UHFFFAOYSA-N triphenoxy(sulfanylidene)-$l^{5}-phosphane Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=S)OC1=CC=CC=C1 IKXFIBBKEARMLL-UHFFFAOYSA-N 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M117/00—Lubricating compositions characterised by the thickener being a non-macromolecular carboxylic acid or salt thereof
- C10M117/02—Lubricating compositions characterised by the thickener being a non-macromolecular carboxylic acid or salt thereof having only one carboxyl group bound to an acyclic carbon atom, cycloaliphatic carbon atom or hydrogen
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M125/00—Lubricating compositions characterised by the additive being an inorganic material
- C10M125/10—Metal oxides, hydroxides, carbonates or bicarbonates
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and additives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M177/00—Special methods of preparation of lubricating compositions; Chemical modification by after-treatment of components or of the whole of a lubricating composition, not covered by other classes
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/06—Metal compounds
- C10M2201/062—Oxides; Hydroxides; Carbonates or bicarbonates
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/06—Metal compounds
- C10M2201/062—Oxides; Hydroxides; Carbonates or bicarbonates
- C10M2201/0626—Oxides; Hydroxides; Carbonates or bicarbonates used as thickening agents
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
- C10M2207/126—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids monocarboxylic
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
- C10M2207/126—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids monocarboxylic
- C10M2207/1265—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids monocarboxylic used as thickening agent
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/283—Esters of polyhydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/02—Groups 1 or 11
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/015—Dispersions of solid lubricants
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/10—Form in which the lubricant is applied to the material being lubricated semi-solid; greasy
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2070/00—Specific manufacturing methods for lubricant compositions
Definitions
- the invention relates to a lithium hydroxide composition, a process for preparing a lithium hydroxide composition, and a process for using a lithium hydroxide composition.
- Soap concentrates for example, lithium soap concentrates, lithium complex soap concentrates, and lithium-calcium complex soap concentrates, may be utilized with a base oil, generally to thicken a base oil, to provide for a lubricating composition commonly referred to as a grease.
- in situ preparation of dilute suspensions of anhydrous lithium hydroxide monohydrate in oil may be useful for preparing soap concentrates and greases.
- the density of solid anhydrous lithium hydroxide is such that the solid tends to settle preventing the formation of a stable suspension comprising lithium hydroxide.
- lithium hydroxide monohydrate is typically dissolved in a solvent such as water. The water must then be removed during the process of preparing the grease. Removing the water consumes time and energy.
- U.S. Pat. No. 5,236,607 to Harris et el. discloses a process for the preparation of a lithium soap thickened grease which consists of heating a mixture of an oil and a lithium base, and optionally also a calcium base, to at least 100° C., then adding a C10-C24 saturated or unsaturated fatty acid, and heating the resulting mixture at a temperature in the range of 110° C. to 200° C. until a thickened grease is obtained.
- WO 2004/031328 A2 discloses a grease composition
- a grease composition comprising a reaction product of a stable dispersion of a metal hydroxide with a number average particle size in the range 20 nanometres to 2 micrometres, a surfactant with a HLB of less than 10, a mono- and/or poly-carboxylic acid, and an oil of lubricating viscosity.
- the method of preparing a grease composition is also disclosed with benefits including a reduction in reaction time, amount of foam produced and environmental hazards.
- a stable lithium hydroxide composition for example, a stable suspension comprising lithium hydroxide, and a process for preparing same, that may be utilized to provide for a soap concentrate or a grease.
- the invention provides for a lithium hydroxide composition
- a lithium hydroxide composition comprising lithium hydroxide, a base oil, and a fatty acid salt.
- the invention also provides for a process for preparing a lithium hydroxide composition comprising contacting a lithium hydroxide component, a base oil, and a fatty acid component.
- the invention also provides for a process of using a lithium hydroxide composition for preparing a soap concentrate comprising contacting the lithium hydroxide composition with a fatty acid component.
- the invention also provides for a process of using a lithium hydroxide composition for preparing a grease comprising contacting the lithium hydroxide composition with a fatty acid component and a base oil.
- the invention provides for a lithium hydroxide composition that may be utilized to provide for a soap concentrate or a grease.
- the invention also provides for the preparing of a lithium hydroxide composition that may be utilized to provide for a soap concentrate or a grease.
- the invention may provide for one or more of the following advantages.
- An advantage of the invention is that a lithium hydroxide composition may be provided that is stable to separation under prolonged storage. In other words, the components of the lithium hydroxide composition do not separate or settle out, for example, during storage.
- Another advantage of the invention is that a stable lithium hydroxide composition may be maintained or stored for a period of time and then used as needed in preparing a soap concentrate or a grease.
- Another advantage of the invention is the flexibility that may be provided by a lithium hydroxide composition of the invention.
- the lithium hydroxide composition may be utilized upon production to further provide for a soap concentrate or a grease, or storing or maintaining the lithium hydroxide composition for future use when needed to provide for a soap concentrate or a grease.
- Another advantage of the invention is that a reduced amount, preferably no amount, of a solvent, for example, water, is added during the preparation of a lithium hydroxide composition of the invention.
- a reduced amount of added solvent may provide for a lithium hydroxide composition that is more dry than a lithium hydroxide composition that is prepared from a process that utilizes an increased amount of solvent that may provide for a reduction in time and energy that is typically required for removing the solvent during, for example, the preparation of a grease.
- a lithium hydroxide composition may be provided that is of a suitable composition that the lithium hydroxide composition may be added to other components to provide for a soap concentrate or a grease.
- a lithium hydroxide composition may be provided using a process of the invention at a particular location. The lithium hydroxide composition may then be relocated to another location for preparing a soap concentrate or a grease.
- a lithium hydroxide composition of the invention comprises lithium hydroxide that includes any suitable form of lithium hydroxide, for example, anhydrous lithium hydroxide, crystalline lithium hydroxide monohydrate, lithium hydroxide monohydrate, or a combination thereof.
- An example lithium hydroxide composition of the invention comprises anhydrous lithium hydroxide and is essentially free of lithium hydroxide monohydrate.
- the anhydrous lithium hydroxide is provided by dehydrating lithium hydroxide monohydrate according to a process of the invention.
- a lithium hydroxide composition of the invention is generally in the form of a suspension comprising lithium hydroxide.
- a lithium hydroxide composition of the invention is preferably in the form of a stable suspension comprising lithium hydroxide.
- a lithium hydroxide composition of the invention comprises particles comprising lithium hydroxide mixed with the other components as described herein.
- the particles comprising lithium hydroxide may be suspended in a base oil.
- stable indicates that a lithium hydroxide composition of the invention comprises a composition that does not readily alter its chemical composition or physical state through storage at ambient conditions.
- the particles comprising lithium hydroxide do not readily separate out of, or settle out of, a lithium hydroxide composition of the invention.
- the particles comprising lithium hydroxide do not readily separate out of, or settle out of, a lithium hydroxide composition of the invention stored under ambient conditions after a time period of 30 days, preferably after a time period of 60 days, and more preferably after a time period of 90 days.
- the term “homogenous” indicates that a lithium hydroxide composition of the invention comprises a substantially uniform structure or composition throughout a lithium hydroxide composition of the invention.
- the stability of a lithium hydroxide composition of the invention provides for the ability to store a lithium hydroxide composition of the invention over long periods of time without a separating out or settling of the components of the lithium hydroxide composition. For example, a time period including from production up to 12 months may be obtained for storing a lithium hydroxide composition of the invention without a significant separating out or settling of the components of the lithium hydroxide composition. Also, for example, a lithium hydroxide composition of the invention may be used upon production as an ingredient for preparing a soap concentrate or a grease. Also, for example, a lithium hydroxide composition of the invention may be used at any time from production up to 12 months.
- a storage time period of greater than 12 months may be obtained.
- a lithium hydroxide composition of the invention may provide for flexibility during processes of preparing a soap concentrate or a grease.
- a lithium hydroxide composition of the invention should not be considered a soap concentrate because the lithium hydroxide, which is generally basic, is generally not neutralized in a lithium hydroxide composition of the invention.
- a lithium hydroxide composition of the invention generally comprises lithium hydroxide in any amount that suitably provides for a lithium hydroxide composition of the invention.
- a lithium hydroxide composition of the invention comprises an amount of lithium hydroxide based on the total weight of the lithium hydroxide composition generally in a range of from 10 weight percent to 60 weight percent, preferably in a range of from 15 weight percent to 50 weight percent, and more preferably in a range of from 20 weight percent to 40 weight percent.
- a lithium hydroxide composition of the invention generally comprises a base oil in any amount that suitably provides for a lithium hydroxide composition of the invention.
- a lithium hydroxide composition of the invention comprises an amount of base oil based on the total weight of the lithium hydroxide composition generally in a range of from 40 weight percent to 90 weight percent, preferably in a range of from 45 weight percent to 85 weight percent, and more preferably in a range of from 50 weight percent to 80 weight percent.
- a lithium hydroxide composition of the invention generally comprises a fatty acid salt in any amount that suitably provides for a lithium hydroxide composition of the invention.
- a fatty acid salt as referred to herein comprises a salt of a fatty acid component as described herein.
- a fatty acid salt is a lithium salt of hydrogenated castor oil fatty acid referred to herein as a castor oil fatty acid lithium salt.
- a lithium hydroxide composition of the invention comprises an amount of fatty acid salt based on the total weight of the lithium hydroxide composition generally in a range of from 0.5 weight percent to 10 weight percent, preferably in a range of from 0.5 weight percent to 9 weight percent, and more preferably in a range of from 1 weight percent to 8 weight percent.
- the fatty acid salt will generally be provided by neutralizing a fatty acid component according to a process of the invention.
- the ratio of water to lithium hydroxide of a lithium hydroxide composition of the invention may be any ratio that suitably provides for a lithium hydroxide composition of the invention.
- the ratio of water to lithium hydroxide is generally in a range of from 0:1 to 7:1, preferably in a range of from 0:1 to 0.75:1, and more preferably in a range of from 0:1 to 0.5:1.
- An advantage of the invention is that a lithium hydroxide composition may be provided without the addition of water. In other words, the ratio of water to lithium hydroxide may be 0:1.
- An additional advantage of the invention includes, but is not limited to, a reduced amount of water being utilized that may provide for a reduction in time and energy needed to dehydrate the resulting mixture comprising a lithium hydroxide component.
- Base oils also referred to in the art as lubricating oils, for use in providing for a lithium hydroxide composition of the invention, a soap concentrate, or a grease may typically be the same as base oils that would normally be selected for oil lubrication.
- the base oil may be of mineral origin, synthetic origin, vegetable origin, animal origin, or a combination thereof.
- Base oils of mineral origin may be mineral oils, for example, those produced by solvent refining or hydroprocessing.
- Base oils of synthetic origin may typically comprise mixtures of C 10 C 50 hydrocarbon polymers, for example liquid polymers of alpha-olefins, ester type polymers, ether type polymers, and combinations thereof.
- Base oils may also include Fischer-Tropsch derived highly paraffinic products.
- the base oil is of mineral origin.
- Suitable examples of synthetic oils include polyolefins such as alpha-olefin oligomers and polybutene, polyalkylene glycols such as polyethylene glycol and polypropylene glycol, diesters such as di-2-ethyl hexyl sebacate and di-2-ethyl hexyl adipate, polyol esters such as trimethylolpropane ester and pentaerythritol ester, perfluorolalkyl ethers, silicone oils, polyphenyl ethers, either individually or as mixed oils.
- polyolefins such as alpha-olefin oligomers and polybutene
- polyalkylene glycols such as polyethylene glycol and polypropylene glycol
- diesters such as di-2-ethyl hexyl sebacate and di-2-ethyl hexyl adipate
- polyol esters such as trimethylolpropane ester
- Examples of base oils suitable for preparing a lithium hydroxide composition of the invention include medium viscosity mineral oils, high viscosity mineral oils, and combinations thereof.
- a base oil suitable for preparing a lithium hydroxide composition of the invention generally has a viscosity in a range of from 2 mm 2 /s centistokes (cSt) at 40° C. to 600 mm 2 /s (cSt) at 40° C., preferably in a range of from 25 mm 2 /s (cSt) at 40° C. to 400 mm 2 /s (cSt) at 40° C., and more preferably in a range of from 50 mm 2 /s (cSt) at 40° C. to 130 mm 2 /s (cSt) at 40° C.
- a medium viscosity mineral oil suitable for preparing a lithium hydroxide composition of the invention may have a viscosity generally in a range of from 95 mm 2 /s centistokes (cSt) at 40° C. to 115 mm 2 /s (cSt) at 40° C., preferably in a range of from 100 mm 2 /s (cSt) at 40° C. to 110 mm 2 /s (cSt) at 40° C., more preferably in a range of from 105 mm 2 /s (cSt) at 40° C.
- cSt centistokes
- a high viscosity mineral oil suitable for preparing a lithium hydroxide composition of the invention may have a viscosity generally in a range of from 120 mm 2 /s (cSt) at 40° C. to 140 mm 2 /s (cSt) at 40° C., preferably in a range of from 125 mm 2 /s (cSt) at 40° C.
- Suitable examples of mineral oils that may be used for preparing a lithium hydroxide composition of the invention include those having the designations “HVI” or “MVI”. Suitable examples include oils having a general designation “MVI 500”, “HVI 250”, or “HVI 600”. Polyalphaolefins and base oils of the type manufactured by the hydroisomerisation of wax may also be used.
- a process of preparing a lithium hydroxide composition of the invention comprises contacting a lithium hydroxide component, a base oil, and a fatty acid component.
- the process generally comprises heating the resulting mixture to dehydrate the lithium hydroxide component to provide for a lithium hydroxide composition of the invention. Heating the resulting mixture may also dehydrate the resulting mixture comprising the lithium hydroxide component.
- the fatty acid component will generally be neutralized during contacting to provide for a fatty acid salt, preferably a castor oil fatty acid lithium salt.
- the lithium hydroxide component is preferably crystalline lithium hydroxide monohydrate.
- Suitable fatty acid components for preparing a lithium hydroxide composition of the invention include fatty acids, fatty acid esters, fatty glycerides, and combinations thereof.
- the fatty acid component comprises carbon atoms generally in a range of from 10 carbon atoms to 24 carbon atoms (C 10 -C 24 ), preferably in a range of from 15 carbon atoms to 18 carbon atoms (C 15 -C 18 ).
- the fatty acid component may be saturated or unsaturated.
- suitable fatty acid components for preparing a lithium hydroxide composition of the invention include oleic acid, palmitic acid, stearic acid, and other carboxylic acids derived from tallow, hydrogenated fish oil, castor oil, wool, grease, and rosin, and combinations thereof.
- suitable fatty acid components for preparing a lithium hydroxide composition of the invention include hydrogenated castor oil (HCO), hydrogenated castor oil fatty acid (HCOFA), and combinations thereof, preferably hydrogenated castor oil fatty acid (HCOFA).
- Hydrogenated castor oil (HCO) is the glyceride of 12-hydroxystearic acid. 12-hydroxystearic acid is a preferred fatty acid.
- Hydrogenated castor oil fatty acid generally comprises at least 85 weight percent of 12-hydroxystearic acid based on the total weight of HCOFA.
- HCOFA may comprise minor amounts of additional components. Examples of additional components include palmitic acid (C16), stearic acid (C18), arachidic acid (C20), 12-ketostearic acid, and combinations thereof.
- HCOFA hydrogenated castor oil fatty acid
- a composition comprising an amount of 12-hydroxystearic acid that provides for a process of the invention, generally an amount comprising at least 85 weight percent 12-hydroxystearic acid based on the total weight of HCOFA, preferably an amount comprising in a range of from 85 to 87 weight percent 12-hydroxystearic acid based on the total weight of HCOFA.
- An example HCOFA that may be used for preparing a lithium hydroxide composition of the invention includes CENWAX A from Arizona Chemical, Jacksonville, Fla., USA.
- Contacting of the components to provide for a lithium hydroxide composition of the invention generally refers to a contacting that is conducted at a temperature, a pressure, and a time period that suitably provides for a lithium hydroxide composition of the invention.
- Contacting generally comprises a heating of the lithium hydroxide component, preferably lithium hydroxide monohydrate, more preferably crystalline lithium hydroxide monohydrate, that provides for a dehydrating of the lithium hydroxide component to provide for a lithium hydroxide composition of the invention. Heating may also provide for a dehydrating of the resulting mixture comprising the lithium hydroxide component.
- a process of the invention comprising a heating and a dehydrating of a lithium hydroxide component may also provide for a heating and a dehydrating of the mixture comprising the lithium hydroxide component.
- Dehydrating may provide for a reduction in time and energy typically required to remove a solvent, for example, water, utilized during the preparation of a soap concentrate or a grease.
- Contacting generally provides for a neutralizing of the fatty acid component with the lithium hydroxide component to provide for a fatty acid salt, for example, a castor oil fatty acid lithium salt.
- Contacting of the components may be conducted in any order that suitably provides for a lithium hydroxide composition of the invention. Contacting of the components may be conducted using any means that suitably provide for a lithium hydroxide composition of the invention. Examples of suitable contacting means include mixing, stirring, circulating, and combinations thereof.
- the temperature during contacting may be any temperature that suitably provides for a heating and a dehydrating of a lithium hydroxide component, a resulting mixture comprising a lithium hydroxide component, or a combination thereof, to provide for a lithium hydroxide composition of the invention and is generally a temperature found in batch processing techniques.
- the temperature is in a range of from 80° C. to 280° C., preferably in a range of from 85° C. to 225° C., and more preferably in a range of from 90° C. to 215° C.
- the pressure during contacting may be any pressure that suitably provides for a heating and a dehydrating of a lithium hydroxide component, a resulting mixture comprising a lithium hydroxide component, or a combination thereof, to provide for a lithium hydroxide composition of the invention and is generally a pressure found in batch processing techniques.
- the pressure is in a range of from atmospheric, in other words, 0 kilopascal (kPa), to 1380 kPa, preferably in a range of from 0 kPa to 690 kPa, and more preferably in a range of from 0 kPa to 345 kPa.
- the time period during contacting may be any time period that suitably provides for a heating and a dehydrating of a lithium hydroxide component, a resulting mixture comprising a lithium hydroxide component, or a combination thereof, to provide for a lithium hydroxide composition of the invention and is generally a time period found in batch processing techniques.
- the time period is in a range of from 0.5 hours to 8 hours, preferably in a range of from 1 hour to 6 hours, and more preferably in a range of from 1 hour to 3 hours.
- a process of preparing a lithium hydroxide composition of the invention may comprise the use of an anti-foaming agent.
- suitable anti-foaming agents include any anti-foaming agent typically used in the art of preparing a soap concentrate or a grease.
- suitable anti-foaming agents for preparing a lithium hydroxide composition of the invention include an anti-foaming agent commercially available from Rhein Chemie under the designation “PC1644”.
- the lithium hydroxide component preferably lithium hydroxide monohydrate, more preferably crystalline lithium hydroxide monohydrate, that is initially present during a process of the invention is dehydrated so that anhydrous lithium hydroxide, also referred to as dehydrated lithium hydroxide, is present in a lithium hydroxide composition of the invention.
- the amount of lithium hydroxide component that is dehydrated to provide for the anhydrous lithium hydroxide based on the total amount of lithium hydroxide component initially present is generally in a range of from 80 percent to 100 percent, preferably in a range of from 90 percent to 100 percent, and more preferably in a range of from 95 percent to 100 percent.
- a lithium hydroxide composition of the invention will generally comprise anhydrous lithium hydroxide and generally no lithium hydroxide monohydrate.
- a lithium hydroxide composition of the invention will comprise anhydrous lithium hydroxide and lithium hydroxide monohydrate.
- Utilizing a process of the invention at different locations may provide for the flexibility to provide for a lithium hydroxide composition of the invention at one location and then send the lithium hydroxide composition to another location to provide for a soap concentrate or a grease depending on the needs of the sent-to location.
- a lithium hydroxide composition of the invention may be prepared utilizing batch processing.
- a lithium hydroxide composition of the invention may be utilized to provide for a soap concentrate or a grease utilizing batch processing, conventional reconstitution techniques, extruder techniques, or a combination thereof.
- a lithium hydroxide composition of the invention may be prepared utilizing batch processing to provide for a resulting lithium hydroxide composition of the invention that may then be utilized to provide for a soap concentrate or a grease utilizing batch processing, conventional reconstitution techniques, extruder techniques, or a combination thereof.
- Batch processing as referred to herein generally comprises the use of one or more large kettles that may be equipped with, for example, paddle agitation, stirring, heating, external recirculation systems capable of pumping the contents from the bottom of the kettle to the top, and combinations thereof.
- Any size kettle that suitably provides for a lithium hydroxide composition of the invention, a soap concentrate, or a grease may be utilized.
- a process of the present invention may be utilized in larger commercial size kettles that may be of a size generally in a range of from 1,000 liters to 20,000 liters, preferably in a range of from 2,000 liters to 15,000 liters, and more preferably in a range of from 3,000 liters to 10,000 liters.
- suitable kettles include open kettles and pressurized kettles.
- An example grease kettle is equipped with stirring, heating, and an external recirculation system, capable of pumping the contents from the bottom of the kettle to the top.
- the reconstitution to provide for a soap concentrate or a grease may take place at the same location(s) as the preparing of a lithium hydroxide composition of the invention or at a different location(s) than the preparing of a lithium hydroxide composition of the invention.
- Storing a lithium hydroxide composition of the invention may be conducted utilizing any temperature and technique used in the art of storing a soap concentrate or a grease. Examples of storing include the use of drums, pails, totes, and combinations thereof, preferably with caustic resistant liners. Storage life may be further increased by storing a lithium hydroxide composition of the invention under an inert atmosphere, for example, nitrogen or argon. A lithium hydroxide composition of the invention is generally allowed to cool prior to storing.
- the temperature of storing a lithium hydroxide composition of the invention may be any temperature that suitably provides for storage. Generally, the temperature is in a range of from 10° C. to 40° C., preferably in a range of from 15° C. to 35° C., and more preferably in a range of from 20° C. to 30° C.
- a soap concentrate prepared utilizing a lithium hydroxide composition of the invention comprises a weight percent of lithium hydroxide composition based on the total weight of soap concentrate generally in a range of from 1 weight percent to 20 weight percent, preferably in a range of from 5 weight percent to 20 weight percent, and more preferably in a range of from 8 weight percent to 15 weight percent.
- Soap concentrates prepared utilizing a lithium hydroxide composition of the invention include simple soap concentrates, complex soap concentrates, and combinations thereof.
- Complex soap concentrates include simple soap concentrates additionally comprising a complexing agent.
- Suitable soap concentrates that may be prepared utilizing a lithium hydroxide composition of the invention include lithium soap concentrates, lithium complex soap concentrates, lithium-calcium soap concentrates, and combinations thereof.
- Examples of preferred soap concentrates prepared utilizing a lithium hydroxide composition of the invention include lithium soap concentrates and lithium complex soap concentrates.
- a soap concentrate for example a lithium soap concentrate, may be prepared by contacting a lithium hydroxide composition of the invention with a fatty acid component as referred to herein. The resulting soap concentrate may then be contacted with a base oil to provide for a grease. Also, for example, a lithium hydroxide composition of the invention may be contacted with a fatty acid component and a base oil to provide for a soap concentrate in situ during the providing of the resulting grease.
- Lithium complex soap concentrates are soap concentrates wherein a complexing agent has been incorporated into a lithium soap concentrate.
- suitable complexing agents include dibasic acids, salts thereof, and combinations thereof, for example azelaic acid, boric acid, lithium borate, and combinations thereof, preferably boric acid.
- a grease prepared utilizing a lithium hydroxide composition of the invention comprises a weight percent of lithium hydroxide composition based on the total weight of grease generally in a range of from 1 weight percent to 20 weight percent, preferably in a range of from 2 weight percent to 15 weight percent, and more preferably in a range of from 2 weight percent to 12 weight percent.
- Examples of greases that may be prepared utilizing a lithium hydroxide composition of the invention include lithium greases, lithium complex greases, lithium-calcium complex greases, and combinations thereof.
- Examples of preferred greases that may be prepared utilizing a lithium hydroxide composition of the invention include lithium greases and lithium complex greases.
- a grease prepared utilizing a lithium hydroxide composition of the invention may comprise additional additives, in amounts normally used in this field of application, to impart certain desirable characteristics to the grease including oxidation stability, tackiness, extreme pressure properties, corrosion inhibition, reduced friction and wear, and combinations thereof.
- suitable additional additives include antioxidants, anti-rust additives, anti-wear and extreme pressure additives, pour point depressants, metal deactivators, and combinations thereof.
- a grease prepared utilizing a lithium hydroxide composition of the invention may comprise from 0.1 weight percent to 10 weight percent, preferably from 0.1 weight percent to 5 weight percent, more preferably from 0.1 weight percent to 2 weight percent, and even more preferably from 0.2 weight percent to 1 weight percent of one or more additional additives as referred to herein based on the total weight of the grease.
- additional additives may be needed to achieve a higher weight percent of additional additive, for example 10 weight percent.
- Suitable additional additives include zinc salts such as zinc dialkyl or diaryl dithiophosphates, borates, molybdenum dithiophosphate, substituted thiadiazoles, polymeric nitrogen/phosphorus compounds made, for example, by reacting a dialkoxy amine with a substituted organic phosphate, amine phosphates, sulphurised sperm oils of natural or synthetic origin, sulphurised lard, sulphurised esters, sulphurised fatty acid esters, sulphurised materials, organophosphates, for example according to the formula (OR) 3 P ⁇ O where R is an alkyl, aryl or aralkyl group, and triphenyl phosphorothionate; one or more overbased metal-containing detergents, such as calcium or magnesium alkyl salicylates, alkylarylsulphonates or alkylsulphonates; ashless dispersant additives, such as reaction products of polyisobutenyl succinic an
- the aryl group is preferably a phenyl group or a naphthyl group.
- the aralkyl group is preferably a benzyl group or methyl naphthenate.
- a grease prepared utilizing a lithium hydroxide composition of the invention may comprise an additional additive comprising a single zinc dithiophosphate or a combination of two or more zinc dithiophosphates.
- a grease prepared utilizing a lithium hydroxide composition of the invention may comprise an additional additive comprising a single ashless dithiocarbamate or a combination of two or more ashless dithiocarbamates.
- HVI high viscosity index
- PC1644 antifoam agent
- the resulting lithium hydroxide composition after dehydration of the lithium hydroxide monohydrate, comprised 36.36 weight percent dehydrated lithium hydroxide, 63.63 weight percent HVI 250 base oil, and 0.01 weight percent PC1644 antifoam agent.
- the resulting lithium hydroxide composition was then transferred to a plastic five-gallon pail. After storage for 24 days at room temperature (70° F. to 80° F.) (21.11° C. to 26.67° C.), the top half of the container contained base oil and the dehydrated lithium hydroxide had settled to the bottom of the pail. After storage for 5 months at room temperature (70° F. to 80° F.) (21.11° C. to 26.67° C.), the appearance was generally the same as after the first 24 days.
- a grease kettle as described herein in EXAMPLE 1 was charged with 5300 grams of medium viscosity index (MVI) mineral oil having a viscosity of 107.87 mm 2 /s (cSt) (500 Saybolt Universal Seconds (SUS)) at 40° C. (104° F.) (generally having a designation “MVI 500”), and 4100 grams of lithium hydroxide monohydrate.
- MVI 500 medium viscosity index
- MVI 500 medium viscosity index
- MVI 500 Saybolt Universal Seconds
- the resulting lithium hydroxide composition after dehydration of the lithium hydroxide monohydrate and neutralization of the HCOFA, comprised 64.20 weight percent (5300 grams) MVI 500 base oil, 28.38 weight percent (2343 grams) dehydrated lithium hydroxide, and 7.41 weight percent (612 grams) castor oil fatty acid lithium salt.
- the resulting mixture was smooth. A portion of the resulting mixture that was run through a three-roll mill had a grease-like consistency. After storing 5000 grams of the resulting lithium hydroxide composition at room temperature (70° F. to 80° F.) (21.11° C. to 26.67° C.) in a five-gallon pail for 5 months, only a slight amount of free oil was observed at the top surface of the pail containing the lithium hydroxide composition.
- a grease kettle as described herein in EXAMPLE 1 was charged with 4700 grams of medium viscosity index (MVI) mineral oil having a viscosity of 107.87 mm 2 /s (cSt) (500 SUS) at 40° C. (104° F.) (generally having a designation “MVI 500”), and 5000 grams of lithium hydroxide monohydrate.
- MVI 500 medium viscosity index
- the resulting mixture was stirred and heated to 190° F. (87.78° C.) at a heating rate of 3° F. (1.667° C.) per minute.
- HCOFA hydrogenated castor oil fatty acid
- the resulting lithium hydroxide composition after dehydration of the lithium hydroxide monohydrate and neutralization of the HCOFA, comprised 59.77 weight percent (4700 grams) MVI 500 base oil, 36.34 weight percent (2857 grams) dehydrated lithium hydroxide, and 3.89 weight percent (306 grams) castor oil fatty acid lithium salt.
- the resulting lithium hydroxide mixture was smooth and somewhat softer than the mixture from EXAMPLE 2. After storing 5000 grams of the resulting lithium hydroxide composition at room temperature (70° F. to 80° F.) (21.11° C. to 26.67° C.) in a five-gallon pail for 12 months, only a slight separation of the components was observed.
- HVI high viscosity index
- cSt 129.46 mm 2 /s
- HVI 600 175.91 grams of the resulting lithium hydroxide composition prepared in EXAMPLE 3.
- the resulting mixture was stirred and heated to 190° F. (87.78° C.) at a heating rate of 3° F. (1.667° C.) per minute.
- 800 grams of hydrogenated castor oil fatty acid (HCOFA) were added to the kettle over a time period of 5 minutes. Heating was resumed at 3° F.
- HVI 600 mineral oil (1.667° C.) per minute to 250° F. (121.1° C.) and 1504 grams of HVI 600 mineral oil were added. Heating and stirring were continued, with heating at 3° F. (1.667° C.) per minute, to 400° F. (204.4° C.). The mixture was stirred for 15 minutes at 400° F. (204.4° C.) and then heating was stopped and 1504 grams of HVI 600 mineral oil were added. The mixture was then stirred and cooled to below 200° F. (93.33° C.) over two hours. An additional 3008 grams of HVI 600 mineral oil were also added during the preparation of the resulting composition. The resulting composition comprised 91.71 weight percent HVI base oil and 8.29 weight percent castor oil fatty acid lithium salt.
- TABLE 1 discloses a summary of various information from EXAMPLES 1-4.
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Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/595,138 US20100273689A1 (en) | 2007-04-13 | 2008-04-10 | Lithium hydroxide composition, a process for preparing a lithium hydroxide composition, and a process for using a lithium hydroxide composition |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US91169507P | 2007-04-13 | 2007-04-13 | |
| PCT/US2008/059828 WO2008127957A1 (fr) | 2007-04-13 | 2008-04-10 | Composition d'hydroxyde de lithium, son procédé de préparation et son procédé d'utilisation |
| US12/595,138 US20100273689A1 (en) | 2007-04-13 | 2008-04-10 | Lithium hydroxide composition, a process for preparing a lithium hydroxide composition, and a process for using a lithium hydroxide composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20100273689A1 true US20100273689A1 (en) | 2010-10-28 |
Family
ID=39625533
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US12/595,138 Abandoned US20100273689A1 (en) | 2007-04-13 | 2008-04-10 | Lithium hydroxide composition, a process for preparing a lithium hydroxide composition, and a process for using a lithium hydroxide composition |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20100273689A1 (fr) |
| EP (1) | EP2152836A1 (fr) |
| JP (1) | JP5587764B2 (fr) |
| CN (2) | CN101679896A (fr) |
| AR (1) | AR067432A1 (fr) |
| BR (1) | BRPI0810156A2 (fr) |
| RU (1) | RU2492216C2 (fr) |
| WO (1) | WO2008127957A1 (fr) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2305781A1 (fr) * | 2009-09-17 | 2011-04-06 | Rhein Chemie Rheinau GmbH | Procédé de fabrication anhydre de graisses de savon au lithium ou au calcium |
| CN103603028B (zh) * | 2013-11-21 | 2016-01-13 | 东北大学 | 一种制备氧化锂或单晶氢氧化锂的方法 |
| RU2669944C1 (ru) * | 2017-11-28 | 2018-10-17 | Публичное акционерное общество "КАМАЗ" | Противоизносная композиция к смазочным маслам |
| CN110257133A (zh) * | 2019-07-03 | 2019-09-20 | 浙江摩路新材料有限公司 | 一种酯类油锂基润滑脂的制备方法 |
| CN112216834B (zh) * | 2020-10-29 | 2021-08-03 | 湖南永杉锂业有限公司 | 一种喷雾包覆制备改性无水氢氧化锂的方法 |
| CN116064185B (zh) * | 2021-10-29 | 2024-12-06 | 中国石油化工股份有限公司 | 制备润滑脂的方法及其应用 |
| CN114106908A (zh) * | 2021-12-22 | 2022-03-01 | 新乡市恒星科技有限责任公司 | 一种石墨高温合成润滑脂及其制备方法 |
| CN115651734A (zh) * | 2022-10-24 | 2023-01-31 | 东莞市欧迪斯润滑剂科技有限公司 | 一种抗磨损的硅油复合锂基润滑脂及其制备工艺 |
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|---|---|---|---|---|
| US2434539A (en) * | 1945-12-22 | 1948-01-13 | Standard Oil Dev Co | Lubricants |
| US2684944A (en) * | 1952-06-02 | 1954-07-27 | Standard Oil Co | Lithium polyorgano siloxane polymer grease compositions |
| US2697693A (en) * | 1951-11-05 | 1954-12-21 | Standard Oil Co | Manufacture of lithium hydroxy carboxylic acid soap greases |
| US4211662A (en) * | 1978-06-06 | 1980-07-08 | Pennwalt Corporation | Synergistic lubricating compositions |
| US4337209A (en) * | 1979-02-14 | 1982-06-29 | Internationale Octrooi Maatschappij "Octropa" B.V. | Process for the manufacture of soap |
| US4597881A (en) * | 1983-05-10 | 1986-07-01 | Idemitsu Kosan Company Limited | Process for producing a lithium-soap grease |
| US5236607A (en) * | 1991-01-15 | 1993-08-17 | Shell Oil Company | Preparation of lithium soap thickened greases |
| US5391309A (en) * | 1991-12-09 | 1995-02-21 | Exxon Research And Engineering Company | Method of preparing high dropping point lithium complex soap greases |
| US6399801B1 (en) * | 2000-05-04 | 2002-06-04 | Lithchem International | Dry powder lithium carboxylates |
| WO2004031328A2 (fr) * | 2002-10-01 | 2004-04-15 | The Lubrizol Corporation | Emulsions deshydratees d'hydroxyde metallique utilisees dans la preparation de graisse |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU973601A1 (ru) * | 1981-05-26 | 1982-11-15 | Ленинградский Ордена Ленина Политехнический Институт Им.М.И.Калинина | Пластична смазка дл т говых цепей |
| RU2048507C1 (ru) * | 1992-06-15 | 1995-11-20 | Общество с ограниченной ответственностью Фирма "Экохимт" | Пластичная смазка |
| JP3561292B2 (ja) * | 1994-07-08 | 2004-09-02 | 協同油脂株式会社 | 生分解性グリース組成物 |
| US6100226A (en) * | 1998-05-20 | 2000-08-08 | The Lubrizol Corporation | Simple metal grease compositions |
| JP5013628B2 (ja) * | 1999-02-09 | 2012-08-29 | 昭和シェル石油株式会社 | ボールジョイント用グリース組成物 |
| JP2000239685A (ja) * | 1999-02-23 | 2000-09-05 | Showa Shell Sekiyu Kk | 等速ジョイント用グリース組成物 |
| US8123823B2 (en) * | 2004-03-31 | 2012-02-28 | The Lurbizol Corporation | High solids content dispersions |
| CN100572509C (zh) * | 2004-03-31 | 2009-12-23 | 卢布里佐尔公司 | 高固体含量的分散体 |
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2008
- 2008-04-10 WO PCT/US2008/059828 patent/WO2008127957A1/fr not_active Ceased
- 2008-04-10 EP EP08745438A patent/EP2152836A1/fr not_active Withdrawn
- 2008-04-10 RU RU2009141850/04A patent/RU2492216C2/ru not_active IP Right Cessation
- 2008-04-10 BR BRPI0810156-6A2A patent/BRPI0810156A2/pt active Search and Examination
- 2008-04-10 JP JP2010503194A patent/JP5587764B2/ja not_active Expired - Fee Related
- 2008-04-10 AR ARP080101479A patent/AR067432A1/es unknown
- 2008-04-10 CN CN200880015305A patent/CN101679896A/zh active Pending
- 2008-04-10 CN CN201510381194.9A patent/CN105132078A/zh active Pending
- 2008-04-10 US US12/595,138 patent/US20100273689A1/en not_active Abandoned
Patent Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2434539A (en) * | 1945-12-22 | 1948-01-13 | Standard Oil Dev Co | Lubricants |
| US2697693A (en) * | 1951-11-05 | 1954-12-21 | Standard Oil Co | Manufacture of lithium hydroxy carboxylic acid soap greases |
| US2684944A (en) * | 1952-06-02 | 1954-07-27 | Standard Oil Co | Lithium polyorgano siloxane polymer grease compositions |
| US4211662A (en) * | 1978-06-06 | 1980-07-08 | Pennwalt Corporation | Synergistic lubricating compositions |
| US4337209A (en) * | 1979-02-14 | 1982-06-29 | Internationale Octrooi Maatschappij "Octropa" B.V. | Process for the manufacture of soap |
| US4597881A (en) * | 1983-05-10 | 1986-07-01 | Idemitsu Kosan Company Limited | Process for producing a lithium-soap grease |
| US5236607A (en) * | 1991-01-15 | 1993-08-17 | Shell Oil Company | Preparation of lithium soap thickened greases |
| US5391309A (en) * | 1991-12-09 | 1995-02-21 | Exxon Research And Engineering Company | Method of preparing high dropping point lithium complex soap greases |
| US6399801B1 (en) * | 2000-05-04 | 2002-06-04 | Lithchem International | Dry powder lithium carboxylates |
| WO2004031328A2 (fr) * | 2002-10-01 | 2004-04-15 | The Lubrizol Corporation | Emulsions deshydratees d'hydroxyde metallique utilisees dans la preparation de graisse |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2008127957A1 (fr) | 2008-10-23 |
| JP5587764B2 (ja) | 2014-09-10 |
| EP2152836A1 (fr) | 2010-02-17 |
| CN101679896A (zh) | 2010-03-24 |
| JP2010523804A (ja) | 2010-07-15 |
| WO2008127957A9 (fr) | 2009-10-22 |
| RU2009141850A (ru) | 2011-05-20 |
| BRPI0810156A2 (pt) | 2014-12-30 |
| RU2492216C2 (ru) | 2013-09-10 |
| AR067432A1 (es) | 2009-10-14 |
| CN105132078A (zh) | 2015-12-09 |
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